(2S,2'S)-2,2'-(Hexadecanedioylbis(azanediyl))dipentanedioic+acid
Supplier:
Strem Chemicals Inc
Description:
BPE, DUPHOS
Supplier:
AMBEED, INC
Description:
(1S,2S)-N,N'-Dimethyl-N,N'-bis(3,3-dimethylbutyl)cyclohexane-1,2-diamine 97%
Catalog Number:
(76075-940)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000 For IHC-P starting dilution is: 1:10~50 For FACS starting dilution is: 1:10~50
Catalog Number:
(76986-494)
Supplier:
AMBEED, INC
Description:
(S)-2-Benzylmorpholine, Purity: 95%, CAS number: 947687-18-5, Appearance: Liquid, Storage: Keep in dark place, Inert atmosphere, 2-8C, Size: 1G
Catalog Number:
(102891-976)
Supplier:
Matrix Scientific
Description:
(2S, 5R)-Tert-Butyl 2, 5-Dimethylpiperazine-1-Carboxylate Hydrochloride, MF=C11H23CLN2O2, MW=250.77, CAS=548762-66-9, 1G
Catalog Number:
(76068-244)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000 For IHC-P starting dilution is: 1:10~50
Supplier:
AMBEED, INC
Description:
(2S)-Isopropyl 2-(((perfluorophenoxy)(phenoxy)phosphoryl)amino)propanoate, Purity: 95%, CAS Number: 1256490-52-4, Appearance: Solid, Storage: Inert atmosphere, 2-8 C, Size: 10g
Supplier:
Strem Chemicals Inc
Description:
BPE, DUPHOS
Supplier:
AMBEED, INC
Description:
(1S,2S)-N1,N1-Dimethylcyclohexane-1,2-diamine 98%
Catalog Number:
(10280-436)
Supplier:
Bioss
Description:
The apolipoprotein L gene family maps to a region on chromosome 22 and encodes six highly homologous proteins designated apoL-I, apoL-II, apoL-III, apoL-IV, apoL-V and apoL-VI, all of which function as components of plasma lipoproteins. ApoL-IV (apolipoprotein L-IV), also known as APOL4, is a 351 amino acid protein that exists as multiple alternatively spliced isoforms, one of which is secreted. Expressed in spleen, placenta, spinal cord, uterus, testis and trachea, apoL-IV is thought to play a role in lipid exchange and transport throughout the body and may be involved in reverse cholesterol transport, specifically from peripheral cells to the liver. Overexpression of apoL-IV is associated with schizophrenia, suggesting that apoL-IV may play a role in the pathogenesis of neural disorders.
Catalog Number:
(10314-306)
Supplier:
Bioss
Description:
C9orf21 (chromosome 9 open reading frame 21) is a 226 amino acid protein that belongs to the UPF0308 family and is encoded by a gene that maps to human chromosome 9q22.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number:
(10318-290)
Supplier:
Bioss
Description:
C9orf139 (chromosome 9 open reading frame 139) is a 190 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number:
(10314-238)
Supplier:
Bioss
Description:
C9orf30 is a 275 amino acid protein that is expressed in brain and belongs to the UPF0439 family. The gene encoding C9orf30 maps to human chromosome 9q31.1. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Supplier:
AMBEED, INC
Description:
(1S,2S)-N,N'-Dimethyl-1,2-diphenylethane-1,2-diamine, Purity: 97%, CAS Number: 70749-06-3, Appearance: Solid or liquid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 25g
Supplier:
Strem Chemicals Inc
Description:
Jacobsen Ligand
Catalog Number:
(PI21331)
Supplier:
Invitrogen
Description:
Thermo Scientific EZ-Link Sulfo-NHS-SS-Biotin is a water-soluble, NHS-ester biotinylation reagent whose spacer arm includes a cleavable disulfide bond for reversible labeling of proteins and cell surface primary amines.
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